Search results for egf

1791 hits were found for egf

# Family MCID Name MIFTS Score
1
c HYP302 Hypomagnesemia 4, Renal 36 45.705
2
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 22 39.321
3
P LNG032 Lung Cancer 98 23.526
4
P CLR023 Colorectal Cancer 100 23.352
5
P BRS047 Breast Cancer 97 21.159
6
P HPT023 Hepatocellular Carcinoma 95 20.833
7
P PNC035 Pancreatic Cancer 86 20.564
8
P OVR042 Ovarian Cancer 88 19.074
9
P GST053 Gastric Cancer 82 17.696
10
GLB002 Glioblastoma 67 17.594
11
P PRS040 Prostate Cancer 95 17.415
12
END057 Endometrial Cancer 71 17.196
13
P BLD134 Bladder Cancer 79 17.144
14
SQM006 Squamous Cell Carcinoma 59 16.428
15
GLM045 Glioma 62 15.284
16
P ADN016 Adenocarcinoma 63 14.814
17
DPH001 Diphtheria 59 14.510
18
CHL014 Cholera 62 13.140
19
ESP021 Esophageal Cancer 84 12.871
20
P PHC003 Pheochromocytoma 70 12.744
21
GST023 Gastric Ulcer 52 12.686
22
P PLY014 Polycystic Kidney Disease 71 12.523
23
P PSR002 Psoriasis 63 12.472
24
RNL114 Renal Cell Carcinoma, Nonpapillary 79 12.429
25
CHR074 Choriocarcinoma 46 12.357
26
BRN028 Brain Cancer 73 11.761
27
INS024 Insulin-Like Growth Factor I 77 11.675
28
PRN019 Perinatal Necrotizing Enterocolitis 60 11.644
29
CLN015 Colon Adenocarcinoma 64 11.575
30
P MLN008 Melanoma 75 11.551
31
PNC129 Pancreatic Adenocarcinoma 65 11.539
32
P LNG064 Lung Cancer Susceptibility 3 70 11.459
33
HGH043 High Grade Glioma 46 11.450
34
LMY002 Leiomyoma 51 11.408
35
P SHR001 Short Bowel Syndrome 53 11.342
36
c FML021 Familial Hypercholesterolemia 71 11.205
37
SQM013 Squamous Cell Carcinoma, Head and Neck 75 10.925
38
P BRS044 Breast Adenocarcinoma 58 10.866
39
BRS050 Breast Cyst 38 10.837
40
CHL122 Cholesteatoma of Middle Ear 51 10.767
41
P CYS039 Cystic Kidney Disease 52 10.579
42
OST159 Osteogenic Sarcoma 66 10.563
43
P NRB001 Neuroblastoma 66 10.307
44
ADN011 Adenoid Cystic Carcinoma 68 10.280
45
PRS045 Prostatic Hypertrophy 52 10.268
46
c ACT071 Acute Kidney Failure 60 10.151
47
MNN043 Meningioma, Familial 79 10.096
48
FCT007 Factor Vii Deficiency 64 10.048
49
CHR100 Chronic Ulcer of Skin 57 9.956
50
P KDN017 Kidney Cancer 60 9.870
51
MCS002 Mucositis 55 9.802
52
HYD002 Hydronephrosis 58 9.800
53
MRF001 Marfan Syndrome 76 9.710
54
GST092 Gastroesophageal Reflux 60 9.703
55
P SKN015 Skin Carcinoma 71 9.673
56
P CYS018 Cystitis 59 9.661
57
P INT143 Interstitial Cystitis 59 9.650
58
P SCH015 Schizophrenia 74 9.559
59
P BLD062 Bile Duct Cancer 68 9.434
60
P HRD020 Hereditary Renal Cell Carcinoma 33 9.299
61
END041 Endometrial Adenocarcinoma 63 9.268
62
c HMP004 Hemophilia B 68 9.218
63
CLR109 Colorectal Adenocarcinoma 50 9.145
64
P CRV031 Cervical Adenocarcinoma 48 9.131
65
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 65 9.075
66
P MDL005 Medulloblastoma 75 9.039
67
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 9.034
68
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 9.019
69
URN010 Urinary Tract Obstruction 55 9.003
70
P ATS364 Autism 72 8.991
71
FLL008 Folliculitis 45 8.951
72
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 8.908
73
OBS082 Obstructive Nephropathy 41 8.900
74
P ATR005 Atrophic Gastritis 50 8.749
75
P DBT009 Diabetes Mellitus 67 8.739
76
BRS051 Breast Disease 58 8.723
78
GNG012 Gingival Overgrowth 49 8.669
79
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 8.612
80
P CTR002 Cataract 59 8.612
81
TNG009 Tongue Squamous Cell Carcinoma 43 8.583
82
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 8.564
83
P INF037 Inflammatory Bowel Disease 53 8.543
84
P AXN002 Axenfeld-Rieger Syndrome 62 8.384
85
P EST001 Estrogen-Receptor Positive Breast Cancer 49 8.354
86
c HYP595 Hypertension, Essential 84 8.354
87
PNC013 Pancreatic Ductal Carcinoma 48 8.354
88
CHL067 Cholecystitis 59 8.270
89
BLD130 Bladder Exstrophy 44 8.256
90
FRN039 Frank-Ter Haar Syndrome 53 8.241
91
P EYD002 Eye Disease 57 8.195
92
TRC008 Trachoma 53 8.186
93
DCT002 Ductal Carcinoma in Situ 58 8.134
94
EST002 Estrogen-Receptor Negative Breast Cancer 45 8.101
95
DNH001 Donohue Syndrome 60 7.986
96
ZLL002 Zollinger-Ellison Syndrome 55 7.940
97
ACT119 Acute Promyelocytic Leukemia 62 7.930
98
THY121 Thyroid Gland Anaplastic Carcinoma 66 7.898
99
CLN044 Colon Adenoma 44 7.886
100
GLN010 Glanzmann Thrombasthenia 66 7.862
101
P OST002 Osteoporosis 77 7.862
102
c ATM101 Autoimmune Gastritis 40 7.849
103
DRY001 Dry Eye Syndrome 49 7.849
104
P HMC002 Homocystinuria 52 7.771
105
DRR016 Diarrhea 2, with Microvillus Atrophy 54 7.752
106
TST014 Testicular Cancer 51 7.752
107
CRB036 Cerebral Meningioma 35 7.729
108
CST001 Costello Syndrome 68 7.702
109
ANL022 Anal Fistula 47 7.702
110
XNT001 Xanthogranulomatous Pyelonephritis 30 7.702
111
P CNR004 Cone-Rod Dystrophy 2 75 7.668
112
END081 Endosteal Hyperostosis, Autosomal Dominant 54 7.668
113
P ALP004 Alport Syndrome 70 7.668
114
MLD006 Mal De Meleda 44 7.584
115
P FRD001 Friedreich Ataxia 62 7.584
116
MLG169 Malignant Astrocytoma 57 7.134
117
P INS002 in Situ Carcinoma 53 7.072
118
c SML038 Small Cell Cancer of the Lung 69 6.880
119
c LKM061 Leukemia, Acute Myeloid 83 6.709
120
SKN019 Skin Melanoma 70 6.578
121
SPP011 Suppression of Tumorigenicity 12 61 6.515
122
c CHR711 Chronic Asthma 41 6.501
123
P ADM011 Adams-Oliver Syndrome 59 6.397
124
RSP023 Rasopathy 54 6.268
125
THY123 Thyroid Gland Follicular Carcinoma 53 6.249
126
PLM134 Pulmonary Fibrosis, Idiopathic 76 6.173
127
P RTN008 Retinitis Pigmentosa 79 6.122
128
GLS001 Gliosarcoma 63 6.076
129
CLC064 Calcifying Aponeurotic Fibroma 22 6.049
130
HYP063 Hypersplenism 52 5.985
131
INT253 Intestinal Benign Neoplasm 46 5.960
132
GLL048 Glial Tumor 52 5.834
133
P PRP019 Peripheral Nervous System Disease 57 5.738
134
THR035 Thrombasthenia 48 5.641
135
FND002 Fundus Dystrophy 55 5.641
136
DYN002 Doyne Honeycomb Retinal Dystrophy 44 5.628
137
HNN001 Hennekam Syndrome 52 5.614
138
P ALG028 Alagille Syndrome 1 73 5.585
139
PLM196 Pulmonary Adenocarcinoma in Situ 34 5.550
140
ADM013 Adamantinoma of Long Bones 34 5.530
141
c ECT098 Ectopia Lentis 1, Isolated, Autosomal Dominant 38 5.481
142
CRB033 Cerebral Degeneration 36 5.481
143
GRV012 Grover's Disease 29 5.481
144
P MTC003 Metachromatic Leukodystrophy 71 5.363
145
P PLZ001 Pelizaeus-Merzbacher Disease 65 5.363
146
c HYP507 Hypotrichosis 1 43 5.363
147
P DST002 Distal Arthrogryposis 63 5.363
148
ATS009 Autosomal Genetic Disease 24 5.363
149
c DFN274 Deafness, Autosomal Dominant 56 34 5.363
150
SRS007 Sorsby Fundus Dystrophy 51 5.363
151
c ECT101 Ectopia Lentis 2, Isolated, Autosomal Recessive 38 5.363
152
THR011 Thoracic Benign Neoplasm 28 5.363
153
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 5.363
154
c PRM023 Pre-Malignant Neoplasm 28 5.363
155
BRS046 Breast Benign Neoplasm 28 5.363
156
c HYP562 Hypothyroidism, Congenital, Nongoitrous, 6 38 5.363
157
c AML044 Amelogenesis Imperfecta, Type Ig 53 5.363
158
TNG004 Tongue Disease 43 5.363
159
ADH006 Adhesive Otitis Media 27 5.363
160
DSS008 Disease of Mental Health 74 5.363
161
c INC034 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 1 21 5.363
162
SPN369 Spinal Disease 43 5.363
163
PRL004 Prolapse of Urethra 28 5.363
164
INF039 Infratentorial Cancer 38 5.363
165
ACT016 Actinobacillosis 30 5.363
166
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 5.363
167
HST011 Histoplasmosis 54 5.363
168
P ATN003 Autonomic Nervous System Neoplasm 25 5.363
169
P PRP021 Peripheral Nervous System Neoplasm 37 5.363
170
PNC012 Punctate Epithelial Keratoconjunctivitis 24 5.363
171
CNT033 Central Nervous System Cancer 47 5.363
172
P AML002 Amelogenesis Imperfecta 56 5.363
173
SBC009 Sebaceous Adenoma 36 5.363
174
MXD020 Mixed Cell Adenoma 30 5.363
175
c BRS049 Breast Carcinoma in Situ 50 5.363
176
LNG003 Lung Carcinoma in Situ 36 5.363
177
PYR008 Pyriform Sinus Cancer 31 5.363
178
PRT037 Pertussis 49 4.732
179
ENT011 Enterocolitis 55 4.167
180
CRV035 Cervical Cancer 72 3.685
181
CYT002 Cytokine Deficiency 43 3.596
182
LNG031 Lung Benign Neoplasm 51 3.554
183
48X005 48,xyyy 39 3.412
184
P SPP010 Suppressor of Tumorigenicity 3 51 3.374
185
ORL015 Oral Squamous Cell Carcinoma 43 3.331
186
ADR040 Adrenal Gland Pheochromocytoma 45 3.238
187
c PCH010 Pachyonychia Congenita 3 43 3.224
188
PST011 Pustulosis of Palm and Sole 52 3.092
189
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.960
190
P GLM040 Glioma Susceptibility 1 70 2.894
191
ADN018 Adenoma 58 2.849
192
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.806
193
CLF027 Cleft Palate, Isolated 64 2.790
194
47X002 47,xyy 48 2.772
195
PRS021 Prostatic Adenoma 43 2.642
196
PRS129 Prostatic Hyperplasia, Benign 48 2.637
197
P GST044 Gastritis 55 2.602
198
P PNC044 Pancreatitis 61 2.586
199
HYP266 Hypoxia 56 2.573
200
c MCR133 Microvascular Complications of Diabetes 4 41 2.561
201
c MCR113 Microvascular Complications of Diabetes 3 52 2.561
202
c MCR130 Microvascular Complications of Diabetes 6 41 2.561
203
c MCR120 Microvascular Complications of Diabetes 7 47 2.561
204
EMB004 Embryonal Carcinoma 55 2.558
205
P RTN024 Retinoblastoma 72 2.553
206
THY029 Thyroid Carcinoma 54 2.544
207
P END044 Endometriosis 62 2.541
208
SKN016 Skin Disease 62 2.482
209
ORL011 Oral Cancer 60 2.423
210
PLY150 Polykaryocytosis Inducer 29 2.399
211
c HYP836 Hypercholesterolemia, Familial, 1 73 2.398
212
P NSP012 Nasopharyngeal Carcinoma 60 2.390
213
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.361
214
BNR002 Bone Resorption Disease 47 2.358
215
PTT037 Pituitary Tumors 44 2.349
216
STM007 Stomatitis 52 2.320
217
INT395 Intracranial Meningioma 48 2.301
218
SCR001 Secretory Meningioma 40 2.301
219
LYM002 Lymphoplasmacyte-Rich Meningioma 35 2.301
220
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.282
221
VCC001 Vaccinia 49 2.278
222
SVR004 Severe Combined Immunodeficiency 71 2.270
223
OVR094 Ovarian Epithelial Cancer 39 2.212
224
GTR002 Goiter 52 2.188
225
c PRC016 Pre-Eclampsia 64 2.187
226
P KDN018 Kidney Disease 72 2.171
227
P ESP024 Esophagitis 60 2.161
228
ANX004 Anoxia 40 2.160
229
P OVR082 Overgrowth Syndrome 42 2.157
230
CHL065 Cholangiocarcinoma 58 2.154
231
INT079 Intrahepatic Cholangiocarcinoma 51 2.154
232
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.154
233
P INF032 Infertility 60 2.102
234
LRY018 Laryngeal Squamous Cell Carcinoma 47 2.078
235
CLT003 Colitis 63 2.054
236
TRN018 Transitional Cell Carcinoma 56 1.999
237
PRS047 Prostatitis 58 1.966
238
PPT005 Peptic Ulcer Disease 58 1.955
239
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.922
240
RHB024 Rhabdomyosarcoma 2 65 1.922
241
P PRD008 Periodontitis 64 1.918
242
P GLM007 Glomerulonephritis 59 1.914
243
GST040 Gastric Adenocarcinoma 66 1.913
244
c ACT027 Acute Pancreatitis 60 1.897
245
URT010 Ureteral Obstruction 45 1.876
246
PRM237 Primary Hypomagnesemia 43 1.870
247
PRN014 Paronychia 50 1.847
248
PPL022 Papilloma 53 1.845
249
SQM002 Squamous Cell Papilloma 45 1.823
250
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.823
251
P FBR017 Fibrosarcoma 55 1.820
252
P EXN002 Exanthem 58 1.811
253
c FNC043 Fanconi Anemia, Complementation Group E 62 1.785
254
LNG099 Lung Disease 62 1.777
255
P NRF002 Neurofibromatosis 60 1.720
256
c PRM108 Primary Progressive Multiple Sclerosis 51 1.705
257
P BNG032 Benign Mesothelioma 53 1.672
258
PRT251 Proteinuria, Chronic Benign 58 1.666
259
HLX001 Helix Syndrome 47 1.659
260
AGN016 Aging 54 1.654
261
LVR012 Liver Cirrhosis 62 1.649
262
SPN186 Spinal Cord Injury 61 1.639
263
P BCL017 B-Cell Lymphoma 57 1.638
264
MRF007 Marfanoid Hypermobility Syndrome 50 1.628
265
LMY014 Leiomyoma, Uterine 55 1.625
266
P HMP007 Hemophilia 52 1.622
267
ANG049 Angioedema Induced by Ace Inhibitors 39 1.621
268
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.620
269
P PLM036 Pulmonary Fibrosis 65 1.620
270
RNL077 Renal Fibrosis 46 1.601
271
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 1.582
272
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 1.582
273
P LRY019 Laryngitis 53 1.580
274
P DDN001 Duodenal Ulcer 53 1.564
275
ISC004 Ischemia 61 1.549
276
MYL069 Myeloma, Multiple 77 1.548
277
INS001 Insulinoma 59 1.546
278
c PRM038 Primary Agammaglobulinemia 47 1.540
279
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.529
280
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.526
281
TRT001 Teratocarcinoma 41 1.518
282
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.515
283
P VTR007 Vitreoretinopathy 45 1.515
284
BRS099 Breast Ductal Carcinoma 61 1.504
285
NRL005 Neurilemmoma 60 1.489
286
BRR014 Barrett Esophagus 66 1.475
287
P LYM118 Lymphoma 69 1.474
288
HYP066 Hyperglycemia 60 1.470
289
ATH013 Atherosclerosis Susceptibility 63 1.462
290
ART016 Aortic Aneurysm 69 1.447
291
CRB004 Cerebral Artery Occlusion 46 1.403
292
PPL002 Papillary Carcinoma 46 1.403
293
DRM006 Dermatitis 62 1.403
294
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 1.398
295
ATM095 Autoimmune Disease 61 1.387
296
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.387
297
BRN056 Bronchopulmonary Dysplasia 57 1.380
298
P GRV001 Graves' Disease 54 1.379
299
c PRS130 Prostate Cancer, Hereditary, 8 32 1.359
300
c PRS136 Prostate Cancer, Hereditary, 6 33 1.359
301
CYS001 Cystic Fibrosis 77 1.358
302
P RHB003 Rhabdomyosarcoma 66 1.358
303
BRN071 Brain Injury 50 1.352
304
TTH032 Tooth Size 35 1.346
305
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.344
306
HMN044 Human Immunodeficiency Virus Type 1 76 1.338
307
PLC008 Placenta Disease 49 1.323
308
c LRG001 Large Cell Carcinoma 48 1.316
309
P LPS004 Lupus Erythematosus 61 1.314
310
PPL052 Papillomatosis, Confluent and Reticulated 34 1.310
311
P ATR011 Atrial Fibrillation 66 1.304
312
P RCT021 Rectum Cancer 54 1.304
313
P LMY004 Leiomyosarcoma 62 1.303
314
ACT003 Acute Kidney Tubular Necrosis 46 1.286
315
BRN024 Bronchitis 67 1.286
316
TLN003 Telangiectasis 51 1.284
317
P HYP076 Hyperthyroidism 53 1.281
318
HMZ003 Homozygous Familial Hypercholesterolemia 60 1.281
319
P CNJ013 Conjunctivitis 66 1.279
320
FBR054 Fibroma 44 1.270
321
OVR059 Ovary Adenocarcinoma 49 1.270
322
PPT001 Peptic Esophagitis 51 1.261
323
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.243
324
PLM014 Pleomorphic Adenoma 51 1.237
325
P ACN011 Acne 55 1.232
326
P THY023 Thymoma 64 1.228
327
c THY107 Thymoma, Familial 42 1.228
328
LKP003 Leukoplakia 39 1.228
329
MSC007 Muscle Hypertrophy 64 1.222
330
P DRM053 Dermatitis, Atopic 65 1.214
331
DWN001 Down Syndrome 70 1.214
332
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.213
333
P ADL010 Adult Respiratory Distress Syndrome 71 1.213
334
P ATX030 Ataxia-Telangiectasia 80 1.205
335
P URN019 Urinary Tract Infection 49 1.205
336
HRW001 Hair Whorl 35 1.196
337
P PLM037 Pulmonary Hypertension 69 1.178
338
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 1.178
339
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.173
340
AML029 Ameloblastoma 46 1.173
341
P MLT020 Multiple Sclerosis 79 1.165
342
ART140 Arteries, Anomalies of 52 1.164
343
LPP008 Lipoprotein Quantitative Trait Locus 65 1.164
344
c PRG020 Paragangliomas 3 39 1.164
345
c ATS007 Autism Spectrum Disorder 72 1.159
346
ADN009 Adenosquamous Carcinoma 49 1.159
347
BLD131 Bladder Urothelial Carcinoma 59 1.159
348
P LRY044 Larynx Cancer 53 1.156
349
MLG079 Malignant Pleural Mesothelioma 42 1.156
350
IGG001 Iga Glomerulonephritis 50 1.152
351
P HRP006 Herpes Simplex 65 1.147
352
P PLY011 Polycystic Ovary Syndrome 57 1.146
353
P MYL006 Myeloid Leukemia 60 1.146
354
END086 End Stage Renal Disease 54 1.146
355
P ART021 Arteriosclerosis 53 1.138
356
c DWL002 Dowling-Degos Disease 1 58 1.137
357
P CLC063 Celiac Disease 1 66 1.132
358
c HPT073 Hepatitis C Virus 71 1.132
359
c MST023 Mesothelioma, Malignant 56 1.132
360
P INT068 Intestinal Disease 53 1.132
361
P ECL001 Eclampsia 52 1.132
362
P FML011 Familial Adenomatous Polyposis 71 1.127
363
CRV002 Cervix Uteri Carcinoma in Situ 48 1.125
364
CRV045 Cervical Intraepithelial Neoplasia 38 1.125
365
CLR108 Colorectal Adenoma 63 1.121
366
c HPT016 Hepatitis B 62 1.118
367
P ALP008 Alopecia 53 1.106
368
SFT003 Soft Tissue Sarcoma 57 1.104
369
END062 Endometrial Hyperplasia 48 1.101
370
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.099
371
NWB001 Newborn Respiratory Distress Syndrome 56 1.099
372
P LCH002 Lichen Planus 55 1.099
373
ORL013 Oral Lichen Planus 45 1.099
374
OTT002 Otitis Media 71 1.097
375
CRV038 Cervical Squamous Cell Carcinoma 56 1.097
376
PRS042 Prostate Disease 42 1.097
377
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.090
378
c BSL007 Basal Cell Carcinoma 68 1.090
379
P HNT016 Huntington Disease 73 1.089
380
TRM010 Traumatic Brain Injury 50 1.089
381
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.082
382
c THY102 Thyroid Cancer, Nonmedullary, 2 54 1.075
383
BCT022 Bacterial Infectious Disease 56 1.075
384
P CRN300 Coronary Heart Disease 1 73 1.075
385
P OPN001 Open-Angle Glaucoma 55 1.067
386
P PLT029 Platelet Groups--Ko System 15 1.067
387
P PTT006 Pituitary Adenoma 55 1.063
388
P AST005 Asthma 76 1.059
389
INT066 Interstitial Lung Disease 60 1.059
390
BWN006 Bowen's Disease 32 1.059
391
c SYS001 Systemic Lupus Erythematosus 86 1.057
392
VTM002 Vitamin B12 Deficiency 48 1.051
393
P RHN004 Rhinitis 57 1.051
394
ACR007 Acromegaly 70 1.043
395
P OLG002 Oligodendroglioma 66 1.043
396
ANP005 Anaplastic Astrocytoma 59 1.043
397
P SML001 Small Cell Carcinoma 52 1.040
398
LPD008 Lipid Metabolism Disorder 61 1.034
399
P AGG001 Aggressive Periodontitis 55 1.034
400
c CHR684 Chronic Kidney Disease 74 1.034
401
P RHM011 Rheumatoid Arthritis 81 1.034
402
c HPT001 Hepatitis C 61 1.034
403
c LKM063 Leukemia, Chronic Myeloid 71 1.026
404
MDD018 Middle East Respiratory Syndrome 44 1.017
405
P OVR106 Ovarian Clear Cell Carcinoma 43 1.017
406
PRR004 Preretinal Fibrosis 34 1.017
407
ULC004 Ulcerative Colitis 74 1.017
408
HLC007 Helicobacter Pylori Infection 67 1.016
409
P VSC007 Vascular Disease 62 1.016
410
P DRR001 Diarrhea 55 1.008
411
PRT013 Portal Hypertension 59 1.004
412
PRT036 Peritonitis 65 1.004
413
OLV002 Oliver Syndrome 41 0.999
414
OST003 Osteonecrosis 61 0.999
415
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.999
416
P HYP040 Hypospadias 51 0.999
417
P ECT006 Ectodermal Dysplasia 62 0.999
418
IMM167 Immune Deficiency Disease 77 0.990
419
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.990
420
ALL014 Allergic Encephalomyelitis 34 0.990
421
CHG001 Chagas Disease 65 0.981
422
ANR040 Aneurysm 60 0.981
423
P TXP001 Toxoplasmosis 60 0.975
424
RTR008 Root Resorption 44 0.971
425
c DPH024 Diaphragmatic Hernia, Congenital 64 0.966
426
KRT009 Keratosis 52 0.966
427
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.961
428
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.961
429
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.961
430
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.961
431
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.961
432
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.961
433
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.961
434
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.961
435
THR024 Thrombosis 56 0.961
436
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.961
437
GST050 Gastrointestinal System Disease 55 0.961
438
c MCR115 Microvascular Complications of Diabetes 5 65 0.959
439
P TRT010 Teratoma 50 0.959
440
ADR016 Adrenal Cortical Carcinoma 61 0.952
441
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.952
442
ALL029 Allergic Disease 61 0.952
443
ADR004 Adrenal Cortical Adenocarcinoma 38 0.952
444
P THY032 Thyroiditis 56 0.952
445
P PLM034 Pulmonary Emphysema 58 0.951
446
P SYS005 Systemic Scleroderma 73 0.945
447
OST012 Osteoarthritis 77 0.945
448
HMN047 Human Cytomegalovirus Infection 59 0.940
449
BRN004 Brain Edema 54 0.940
450
c WLM013 Wilms Tumor 1 65 0.931
451
CYS014 Cystadenocarcinoma 51 0.931
452
c PRD040 Periodontitis, Chronic 52 0.929
453
MCP006 Mucoepidermoid Carcinoma 48 0.929
454
DPR016 Depression 65 0.924
455
SLD003 Sialadenitis 47 0.917
456
BRK010 Burkitt Lymphoma 66 0.917
457
P LKM002 Leukemia 66 0.917
458
HPT022 Hepatoblastoma 54 0.917
459
CRH001 Crohn's Disease 80 0.913
460
c ATS393 Autosomal Recessive Cutis Laxa Type I 49 0.912
461
MYL005 Myelofibrosis 70 0.906
462
c INF023 Inflammatory Breast Carcinoma 48 0.906
463
LNT004 Lentigines 45 0.899
464
P TRM003 Tremor 50 0.894
465
CNT047 Contact Dermatitis 57 0.893
466
THY022 Thymic Carcinoma 56 0.893
467
P MJR001 Major Depressive Disorder 68 0.887
468
P ICH004 Ichthyosis 56 0.887
469
MNT002 Mental Depression 56 0.887
470
DMY004 Demyelinating Disease 50 0.887
471
PLR022 Pleural Disease 45 0.880
472
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.879
473
P GLL018 Gallbladder Cancer 53 0.879
474
P CRN024 Corneal Disease 43 0.871
475
GST071 Gastrointestinal Carcinoma 46 0.871
476
P OVR046 Ovarian Cyst 44 0.871
477
P HPT021 Hepatitis 68 0.871
478
PRT014 Protein S Deficiency 46 0.867
479
CHL004 Cholelithiasis 48 0.867
480
c TYP008 Type 1 Diabetes Mellitus 77 0.863
481
CRN027 Corneal Neovascularization 47 0.863
482
P NPH012 Nephrotic Syndrome 62 0.863
483
BLD044 Bladder Disease 48 0.863
484
MST020 Mast Cell Activation Syndrome 27 0.863
485
FTT001 Fatty Liver Disease 61 0.863
486
ACN002 Acanthosis Nigricans 56 0.854
487
CLR030 Clear Cell Renal Cell Carcinoma 54 0.854
488
HYP056 Hypoglycemia 65 0.854
489
c NRF023 Neurofibromatosis, Type Ii 70 0.852
490
THY111 Thyroid Carcinoma, Familial Medullary 67 0.852
491
EWN003 Ewing Sarcoma 70 0.852
492
ECH003 Echinococcosis 52 0.852
493
P FTL001 Fetal Alcohol Syndrome 55 0.846
495
P RTN016 Retinal Degeneration 52 0.846
496
P ANR048 Aniridia 1 66 0.845
497
c PSR023 Psoriasis 1 52 0.845
498
P LKM062 Leukemia, Acute Lymphoblastic 69 0.837
499
c MCR112 Microvascular Complications of Diabetes 2 42 0.837
500
P MCR129 Microvascular Complications of Diabetes 1 68 0.837
501
c MJR024 Major Affective Disorder 9 40 0.837
502
c MJR022 Major Affective Disorder 8 37 0.837
503
HYP060 Hyperinsulinism 53 0.837
504
RTN003 Retinal Ischemia 48 0.837
505
P BPL003 Bipolar Disorder 56 0.837
506
PPL018 Papillary Adenocarcinoma 44 0.837
507
c ACT135 Acute Graft Versus Host Disease 51 0.837
508
HYP014 Hyperuricemia 51 0.837
509
P PMP001 Pemphigus 55 0.828
510
P PNM007 Pneumonia 64 0.827
511
P VSC013 Visceral Heterotaxy 53 0.820
512
THY125 Thyroid Gland Medullary Carcinoma 48 0.820
513
SMN007 Seminoma 42 0.820
514
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.820
515
P BRS053 Breast Fibroadenoma 48 0.819
516
P INF038 Influenza 68 0.819
517
KLD004 Keloid Disorder 39 0.819
518
ORL012 Oral Leukoplakia 35 0.819
519
ALC006 Alcoholic Hepatitis 61 0.811
520
FML037 Female Breast Cancer 51 0.810
521
PMP006 Pemphigus Vulgaris, Familial 58 0.810
522
c DLT002 Dilated Cardiomyopathy 79 0.810
523
c SPN225 Spondyloarthropathy 1 70 0.803
524
SPN051 Spondylitis 51 0.803
525
INF009 Inflammatory Spondylopathy 30 0.803
526
KRT003 Keratinizing Squamous Cell Carcinoma 36 0.803
527
P AMY004 Amyloidosis 69 0.803
528
PLM033 Pulmonary Embolism 58 0.803
529
c TYP009 Type 2 Diabetes Mellitus 92 0.801
530
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.801
531
P PRK039 Parkinsonism 55 0.801
532
CRT015 Carotid Artery Occlusion 45 0.801
533
P HYP098 Hypereosinophilic Syndrome 66 0.801
534
c TBR025 Tuberous Sclerosis 1 84 0.796
535
c WLM018 Wilms Tumor 5 54 0.793
536
CMB007 Combined Immunodeficiency 56 0.791
537
BRN032 Brain Glioma 45 0.791
538
LWC001 Low Compliance Bladder 44 0.791
539
PRN039 Paraneoplastic Syndromes 37 0.791
540
MCR011 Microinvasive Gastric Cancer 41 0.781
541
ALL003 Allergic Rhinitis 66 0.781
542
P NNN008 Noonan Syndrome 1 76 0.781
543
P RSP003 Respiratory Failure 74 0.781
544
ANT024 Anthrax Disease 58 0.781
545
c PSD047 Pseudo-Turner Syndrome 52 0.781
546
c ACT068 Acute Cystitis 61 0.770
547
P USH001 Usher Syndrome 64 0.760
548
BLR013 Biliary Tract Cancer 43 0.760
549
PLC005 Placental Insufficiency 56 0.760
550
P EPD016 Epidermolysis Bullosa 53 0.760
551
BNN003 Bone Inflammation Disease 47 0.760
552
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 0.749
553
ATS010 Autosomal Recessive Disease 42 0.749
554
MLD018 Mild Cognitive Impairment 48 0.749
555
NRR001 Neuroretinitis 42 0.749
556
KPS004 Kaposi Sarcoma 76 0.749
557
NRL016 Neural Tube Defects 81 0.749
558
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.749
559
LYD001 Leydig Cell Tumor 45 0.749
560
TXC005 Toxic Shock Syndrome 62 0.749
561
TTN003 Tetanus 64 0.749
562
RTN023 Retinitis 45 0.749
563
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.749
564
MSL001 Measles 61 0.749
565
c LKM005 Leukemia, T-Cell, Chronic 33 0.749
566
MD2001 Med23 18 0.749
567
RCK004 Rickets 65 0.737
568
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.737
569
NDL007 Nodular Goiter 48 0.737
570
P ART023 Arthropathy 60 0.737
571
ACT058 Active Peptic Ulcer Disease 55 0.737
572
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.737
573
P MNC007 Monocytic Leukemia 48 0.737
574
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.734
575
PLY024 Polymicrogyria 46 0.734
576
c PSR032 Psoriasis 11 47 0.726
577
c PSR018 Psoriasis 13 40 0.726
578
c PSR028 Psoriasis 7 43 0.726
579
ACT011 Acute Contagious Conjunctivitis 42 0.726
580
c PSR017 Psoriasis 2 53 0.726
581
c BRN108 Branchiootic Syndrome 1 63 0.725
582
HPT067 Hepatocellular Adenoma 42 0.725
583
PSR001 Psoriatic Arthritis 61 0.725
584
HPT004 Hepatic Coma 43 0.725
585
ACS001 Acoustic Neuroma 56 0.725
586
MCN001 Mucinous Adenocarcinoma 49 0.725
587
CNG034 Congestive Heart Failure 69 0.725
588
P HMN010 Hemangioma 61 0.725
589
CHN010 Chondroma 43 0.725
590
HPT019 Hepatic Encephalopathy 59 0.725
591
PLM011 Plummer's Disease 34 0.725
592
P TCD001 Tic Disorder 50 0.725
593
APP009 Appendix Adenocarcinoma 47 0.725
594
P CHR345 Chronic Pain 50 0.725
595
P HYP265 Hypotonia 42 0.725
596
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.725
597
c ATR087 Atrial Standstill 1 74 0.713
598
P PRV006 Pervasive Developmental Disorder 52 0.713
599
P KLZ004 Kala-Azar 1 41 0.713
600
P HYD006 Hydrocephalus 63 0.713
601
SKN022 Skin Squamous Cell Carcinoma 54 0.713
602
MMM001 Mammary Paget's Disease 53 0.713
603
LSH001 Leishmaniasis 63 0.713
604
MXD026 Mixed Glioma 45 0.701
605
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 53 0.700
606
DYS018 Dysostosis 43 0.700
607
MST005 Mastitis 52 0.700
608
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.700
609
ORL004 Oral Submucous Fibrosis 56 0.700
610
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.700
611
MYL009 Myelodysplastic Syndrome 67 0.687
612
EST007 Estrogen Resistance 41 0.687
613
LYM157 Lymph Node Carcinoma 33 0.687
614
P SLP006 Sleep Apnea 69 0.687
615
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.687
616
CYS009 Cystadenoma 43 0.687
617
P OBS001 Obstructive Jaundice 49 0.687
618
PLY100 Polyploidy 36 0.687
619
VRC005 Varicose Veins 59 0.672
620
ANK001 Ankylosis 51 0.672
621
RTN020 Retinal Vascular Disease 45 0.672
622
HMS001 Hemosiderosis 48 0.672
623
PNL012 Penile Cancer 57 0.672
624
OST004 Osteitis Fibrosa 38 0.672
625
c CNT035 Central Nervous System Disease 53 0.672
626
P NRV007 Nervous System Disease 66 0.672
627
CTN007 Cutaneous Leishmaniasis 61 0.672
628
P RRH023 Rare Hereditary Hemochromatosis 53 0.672
629
MLG163 Malignant Tumor of Penis 29 0.672
630
c HMC039 Hemochromatosis, Type 1 73 0.657
631
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.657
632
P TTR001 Tetralogy of Fallot 69 0.657
633
P GCH001 Gaucher's Disease 69 0.657
634
c CHR087 Chronic Cystitis 37 0.657
635
HRT011 Heart Septal Defect 49 0.657
636
EST004 Estrogen Excess 37 0.657
637
c CHR057 Chronic Laryngitis 34 0.657
638
P KRT005 Keratoacanthoma 47 0.657
639
P MLT007 Multiple Epiphyseal Dysplasia 55 0.657
640
TRP005 Trophoblastic Neoplasm 39 0.657
641
CLF001 Cleft Lip 54 0.657
642
ALL006 Allergic Asthma 56 0.657
643
P MNN013 Meningitis 65 0.657
645
DSC013 Discrimination, Two-Point, Reduction in 21 0.640
646
GT001 Gout 63 0.640
647
PRP016 Paraplegia 52 0.640
648
c HRD010 Hereditary Spastic Paraplegia 65 0.640
649
CTN004 Cutaneous Fibrous Histiocytoma 39 0.640
650
P ENC004 Encephalitis 61 0.640
651
EPD090 Epidermal Disease 12 0.640
652
MLN065 Melanocytic Nevus Syndrome, Congenital 61 0.633
653
CHR072 Chordoma 57 0.622
654
AST006 Astigmatism 46 0.622
655
P DNG005 Dengue Virus 55 0.622
656
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 48 0.622
657
PRD041 Periodic Fever, Menstrual Cycle-Dependent 23 0.622
658
c VSC019 Vesicoureteral Reflux 1 56 0.622
659
P GRN010 Granular Cell Tumor 40 0.622
660
NNN026 Noonan Syndrome with Multiple Lentigines 65 0.622
661
VSC006 Vascular Cancer 46 0.622
662
RCR001 Recurrent Corneal Erosion 33 0.622
663
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.622
664
CLL005 Cellular Leiomyoma 28 0.622
665
P DBT005 Diabetes Insipidus 54 0.622
666
CLF056 Cleft Lip with or Without Cleft Palate 43 0.622
667
FML292 Familial Drusen 34 0.622
668
SRC014 Sarcoma 64 0.622
669
SPN035 Spindle Cell Sarcoma 51 0.622
670
c SCL052 Scleroderma, Familial Progressive 60 0.617
671
P RTN018 Retinal Disease 53 0.605
672
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.603
673
FCT003 Factor X Deficiency 54 0.603
674
ACH004 Achondroplasia 66 0.603
675
c CLR077 Colorectal Cancer 10 32 0.603
676
P THN009 Thanatophoric Dysplasia, Type I 62 0.603
677
THY006 Thymus Lymphoma 27 0.603
678
TTH002 Tooth Agenesis 61 0.603
679
ART017 Aortic Disease 49 0.603
680
HMN009 Hemangioblastoma 53 0.603
681
P HYP061 Hypertrophic Cardiomyopathy 69 0.603
682
ASB001 Asbestosis 47 0.603
683
MCL006 Macular Retinal Edema 56 0.603
684
P PSD003 Pseudohypoaldosteronism 45 0.603
685
P LPS002 Liposarcoma 64 0.603
686
OVR048 Ovarian Cystadenoma 30 0.603
687
c XRD022 Xeroderma Pigmentosum, Complementation Group D 56 0.603
688
BLS002 Blastomycosis 47 0.603
689
SMT003 Somatostatinoma 52 0.603
690
DBT006 Diabetic Macular Edema 48 0.603
691
HRT036 Heritable Thoracic Aortic Disease 36 0.603
692
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.603
693
ASB003 Asbestos Intoxication 32 0.603
694
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.603
695
P RRT020 Rare Tumor 39 0.603
696
ARG004 Argyria 26 0.599
697
P ANP001 Anaplastic Large Cell Lymphoma 61 0.597
698
c OVR114 Ovarian Cancer 1 60 0.597
699
GST095 Gastritis, Familial Giant Hypertrophic 41 0.597
700
P LNG035 Lung Large Cell Carcinoma 53 0.597
701
P ALZ034 Alzheimer Disease 87 0.583
702
P HYP534 Hypomagnesemia 3, Renal 46 0.580
703
c HTR009 Heterotaxy, Visceral, 2, Autosomal 27 0.580
704
LBR036 Leber Plus Disease 67 0.580
705
INT067 Interstitial Nephritis 47 0.580
706
P LPR012 Leopard Syndrome 1 48 0.580
707
MTC018 Metachondromatosis 48 0.580
708
MYX005 Myxoid Liposarcoma 65 0.580
709
c ADM009 Adams-Oliver Syndrome 4 25 0.580
710
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.580
711
P ESS003 Essential Thrombocythemia 68 0.580
712
IRR003 Irritant Dermatitis 47 0.580
713
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 34 0.580
714
c SPR009 Sporadic Breast Cancer 42 0.580
716
HTR003 Heterotaxy 44 0.580
717
GLC036 Glucagonoma 45 0.580
718
CLP005 Ciliopathy 41 0.580
719
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.557
720
c ACT134 Acute Liver Failure 57 0.557
721
DNY001 Denys-Drash Syndrome 57 0.553
722
ICH020 Ichthyosis Prematurity Syndrome 40 0.553
723
URL001 Urolithiasis 45 0.553
724
SPN250 Spondyloepimetaphyseal Dysplasia 35 0.553
725
DSM004 Desmoid Tumor 65 0.553
726
c OPT053 Optic Atrophy 1 62 0.553
727
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.553
728
PST010 Pasteurellosis 38 0.553
729
ALV002 Alveolar Echinococcosis 56 0.553
730
TST018 Testicular Yolk Sac Tumor 39 0.553
731
P END039 Endodermal Sinus Tumor 42 0.553
732
ALL010 Allergic Contact Dermatitis 56 0.553
733
PLC003 Placental Site Trophoblastic Tumor 45 0.553
734
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.553
735
NNS011 Nonseminomatous Germ Cell Tumor 33 0.553
736
P MYC033 Myoclonus 46 0.553
737
UND009 Undifferentiated Carcinoma of Stomach 17 0.553
738
P TBR001 Tuberous Sclerosis 69 0.544
739
P ALC033 Alcohol Use Disorder 67 0.537
740
P WSK001 Wiskott-Aldrich Syndrome 72 0.524
741
ART001 Arterial Tortuosity Syndrome 64 0.519
742
P STS008 Sotos Syndrome 1 62 0.519
743
CHL147 Chlamydia Pneumonia 47 0.519
744
KLD003 Keloid Formation 34 0.519
745
GNT002 Giant Cell Glioblastoma 57 0.519
746
P ATR010 Atrial Heart Septal Defect 58 0.519
747
CHL123 Chlamydia 58 0.519
748
TCK004 Tick Infestation 29 0.519
749
OCL006 Ocular Hypertension 53 0.519
750
c PNS012 Paine Syndrome 60 0.513
751
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.513
752
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.513
753
ATN011 Autoinflammation with Infantile Enterocolitis 46 0.513
754
SPL004 Splenic Marginal Zone Lymphoma 50 0.513
755
c FML001 Familial Atrial Fibrillation 65 0.513
756
P LYM033 Lymphoproliferative Syndrome 59 0.513
757
c FML347 Familial Adenomatous Polyposis 2 56 0.513
758
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.513
759
FLL027 Fallopian Tube Carcinoma 66 0.513
760
SML008 Small Intestine Lymphoma 33 0.513
761
PRT035 Peritoneum Cancer 45 0.513
762
CLN045 Colonic Benign Neoplasm 48 0.513
763
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.513
764
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.513
765
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 0.513
766
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 0.513
767
PST046 Post-Transplant Lymphoproliferative Disease 53 0.513
768
AND005 Androgen Insensitivity Syndrome, Mild 21 0.513
769
INT054 Intraocular Lymphoma 48 0.513
770
LYM019 Lymphosarcoma 46 0.513
771
P PRK057 Parkinson Disease, Late-Onset 79 0.510
772
RTN017 Retinal Detachment 60 0.510
773
ACT098 Acute Erythroid Leukemia 55 0.496
774
P MYP006 Myopia 55 0.496
775
VLV032 Vulva Cancer 60 0.496
776
P HYP069 Hyperparathyroidism 62 0.496
777
P MMB011 Membranous Nephropathy 50 0.489
778
MSN004 Mesenchymal Cell Neoplasm 42 0.489
779
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.475
780
c MLG084 Malignant Fibrous Histiocytoma 62 0.475
781
GST010 Gestational Trophoblastic Neoplasm 52 0.475
782
P GRF003 Graft-Versus-Host Disease 71 0.467
783
TNG007 Tongue Carcinoma 55 0.467
784
KRT008 Keratopathy 46 0.467
785
LNG039 Lung Squamous Cell Carcinoma 57 0.467
786
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.460
787
P PRL003 Proliferative Glomerulonephritis 43 0.460
788
P LTR001 Lateral Sclerosis 58 0.460
789
P HYP086 Hypothyroidism 69 0.460
790
P FBR003 Fibrous Histiocytoma 43 0.452
791
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.444
792
P MSC005 Muscular Dystrophy 66 0.444
793
THY128 Thyroid Tumor 33 0.444
794
OCL069 Ocular Motor Apraxia 57 0.435
795
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.435
796
P SPN301 Spinocerebellar Ataxia 2 59 0.435
797
c INF002 Inflammatory Diarrhea 30 0.435
798
CRY001 Cryptogenic Organizing Pneumonia 53 0.435
799
TTT001 Tatton-Brown-Rahman Syndrome 45 0.435
800
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.435
801
NNS002 Nonspecific Interstitial Pneumonia 42 0.435
802
CRN020 Coronary Restenosis 39 0.435
803
ACN003 Acneiform Dermatitis 35 0.435
804
c BCT006 Bacterial Conjunctivitis 42 0.435
805
SPN050 Spinocerebellar Degeneration 39 0.435
806
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 44 0.435
807
HYP457 Hypertrophic Scars 42 0.428
808
CHR178 Chromosomal Triplication 34 0.428
809
PRP027 Peripheral Vascular Disease 71 0.420
810
HPT070 Hepatosplenic T-Cell Lymphoma 36 0.413
811
P CHN012 Chondrosarcoma 56 0.411
812
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.411
813
CRC014 Carcinoid Tumors, Intestinal 46 0.411
814
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.411
815
NRF007 Neurofibroma 64 0.411
816
FBR019 Fibromatosis 44 0.411
817
MLL001 Molluscum Contagiosum 48 0.411
818
OCC016 Occupational Asthma 33 0.402
819
P FCL005 Focal Segmental Glomerulosclerosis 57 0.402
820
APH001 Aphthous Stomatitis 57 0.402
821
INV018 Invasive Mole 22 0.402
822
P ALP061 Alopecia, Androgenetic, 1 49 0.394
823
AND014 Androgenic Alopecia 46 0.394
824
KRT019 Keratitis, Hereditary 66 0.394
825
c ACT073 Acute Leukemia 59 0.394
826
FLL031 Follicular Adenoma 40 0.394
827
AZS001 Azoospermia 45 0.394
828
MDD011 Mood Disorder 62 0.385
829
GLM044 Glomerular Disease 34 0.385
830
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.375
831
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.375
832
MCN008 Mucinous Cystadenocarcinoma 39 0.375
833
STT009 Sutton Disease 2 29 0.375
834
P NRP001 Neuropathy 59 0.375
835
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.366
836
P HYP009 Hypertrophic Pyloric Stenosis 41 0.366
837
PYL006 Pyloric Stenosis 48 0.366
838
P BND020 Bone Disease 60 0.366
839
CHL068 Cholestasis 61 0.366
840
PRC003 Proctitis 49 0.366
841
VSC002 Vascular Dementia 59 0.366
842
c SPR119 Spermatogenic Failure, X-Linked, 1 36 0.356
843
NNL006 Non-Alcoholic Steatohepatitis 54 0.356
844
c ACT249 Acute Asthma 40 0.356
845
DFC004 Deficiency Anemia 74 0.356
846
STR067 Stroke, Ischemic 79 0.356
847
P ENC018 Encephalopathy 62 0.356
848
KRT006 Keratoconjunctivitis 53 0.356
849
NRT011 Neurotrophic Keratopathy 36 0.356
850
SYN007 Synovitis 54 0.346
851
PLC002 Plica Syndrome 35 0.346
852
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.346
853
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.336
854
P MLN069 Melanoma, Uveal 59 0.336
855
KRT001 Keratoconjunctivitis Sicca 49 0.336
856
P ANT006 Antiphospholipid Syndrome 55 0.336
857
P BNG030 Benign Ependymoma 51 0.336
858
PCD001 Pica Disease 38 0.336
859
THR004 Thrombocytosis 52 0.336
860
PRP030 Purpura 54 0.336
861
CLL010 Cellular Ependymoma 58 0.336
862
c GLL024 Gallbladder Disease 1 53 0.325
863
CHR005 Chorioamnionitis 50 0.325
864
ALC007 Alcohol Dependence 65 0.325
865
P GNG025 Gingival Fibromatosis 46 0.325
866
BLR001 Biliary Atresia 55 0.325
867
VRC001 Varicocele 48 0.325
868
SRS001 Serous Cystadenocarcinoma 51 0.325
869
ANG018 Angiomyolipoma 45 0.325
870
P SZR006 Seizure Disorder 69 0.325
871
DFF036 Differentiated Thyroid Carcinoma 51 0.325
872
BNG077 Benign Idiopathic Neonatal Seizures 22 0.325
873
MLG141 Malignant Atrophic Papulosis 35 0.314
874
P MLT008 Multinodular Goiter 42 0.314
875
P DWL001 Dowling-Degos Disease 44 0.314
876
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.314
877
TST044 Testicular Torsion 45 0.314
878
CRB039 Cerebrovascular Disease 65 0.314
879
P THR015 Thrombophilia 51 0.314
880
MXL017 Maxillary Cancer 31 0.314
881
P ART022 Arthritis 70 0.314
882
LWG005 Low-Grade Astrocytoma 38 0.314
883
MLG164 Malignant Epithelial Tumor of Ovary 24 0.314
884
LWG006 Low Grade Glioma 41 0.303
885
LMB062 Limb Ischemia 55 0.303
886
MLR004 Malaria 78 0.303
887
LYM007 Lymphangioleiomyomatosis 68 0.303
888
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.303
889
THY030 Thyroid Gland Disease 50 0.303
890
THY122 Thyroid Gland Cancer 59 0.303
891
c SCN007 Secondary Hyperparathyroidism 51 0.303
892
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 61 0.303
893
CRB090 Cerebral Hypoxia 42 0.303
894
P BRN022 Bronchiectasis 59 0.303
895
ORP003 Oropharynx Cancer 54 0.303
896
c NRB010 Neuroblastoma 1 60 0.292
897
P RNL017 Renal Oncocytoma 54 0.292
898
CHR020 Chronic Interstitial Cystitis 36 0.292
899
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.291
900
WRN001 Werner Syndrome 69 0.291
901
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.291
902
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.291
903
c VRL010 Viral Hepatitis 52 0.291
904
P ISL078 Isolated Ectopia Lentis 58 0.291
905
SVR001 Severe Acute Respiratory Syndrome 68 0.291
906
PLC006 Placental Choriocarcinoma 38 0.291
907
CRB037 Cerebral Palsy 67 0.291
908
NRG002 Neurogenic Bladder 55 0.291
909
SKN005 Skin Atrophy 41 0.291
910
LMB050 Limbal Stem Cell Deficiency 50 0.291
911
MCP033 Mucopolysaccharidoses 44 0.291
912
P ALP009 Alopecia Areata 59 0.291
913
ADN027 Adenomyosis 59 0.278
914
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.278
915
CNT099 Contractural Arachnodactyly, Congenital 54 0.278
916
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.278
917
PRT010 Parathyroid Carcinoma 68 0.278
918
P MYC007 Myocardial Infarction 69 0.278
919
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.278
920
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.278
921
P SJG008 Sjogren Syndrome 61 0.278
922
SRC027 Sarcoma, Synovial 58 0.278
923
P PYL005 Pyelonephritis 56 0.278
924
RHB001 Rhabdoid Cancer 68 0.278
925
MYF001 Myofibroma 42 0.278
926
IRR002 Irritable Bowel Syndrome 65 0.278
927
P PRC019 Precocious Puberty 49 0.278
928
HYP025 Hyperphosphatemia 47 0.265
929
c PSR025 Psoriasis 4 29 0.265
930
HSH003 Hashimoto Thyroiditis 60 0.265
931
c SVR005 Severe Pre-Eclampsia 50 0.265
932
P RPD001 Rapidly Progressive Glomerulonephritis 43 0.265
933
c ESS001 Essential Tremor 56 0.265
934
P BNG095 Benign Giant Cell Tumor 43 0.265
935
P DMN002 Dementia 65 0.265
936
OLG001 Oligospermia 45 0.265
937
P NTR004 Neutropenia 62 0.265
938
P HRT032 Heart Disease 84 0.265
939
VGN019 Vaginal Discharge 47 0.265
940
RST023 Resting Heart Rate, Variation in 40 0.265
941
SGN002 Signet Ring Cell Adenocarcinoma 46 0.265
942
PPL014 Papillary Transitional Carcinoma 25 0.265
943
P MYP004 Myopathy 67 0.265
944
CHR261 Chromosome 7p Duplication 13 0.265
945
c BCT013 Bacterial Pneumonia 47 0.265
946
PRT145 Partial Deletion of Chromosome 3 8 0.265
947
c INH030 Inherited Retinal Disorder 28 0.265
948
c GRV008 Graves Disease 1 54 0.252
949
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.252
950
c MGR033 Migraine with or Without Aura 6 17 0.252
951
P CRD119 Cardiac Arrest 68 0.252
952
P CRN026 Corneal Edema 42 0.252
953
CRT013 Carotid Stenosis 51 0.252
954